Jammin 4 Justin Diabetes Benefit

Jammin 4 JustinJustin Lindstrom was only 11 years old when he lost his battle with type 1 diabetes last summer.  I didn’t know Justin, but I did recently meet his parents, which is how I got to know his story.  Jammin 4 Justin is a benefit and concert to honor his memory.  It is the brainchild of his parents, who now have a passion to do whatever they can to save other children from this terrible disease.  His father is a member of a Quad City area band that you might remember from the 90’s, called Crop Circle which is still performing today.

I have had type 1 diabetes since 1970, and as a child, there were far to many nights where my parents would awaken to me having seizures due to low blood sugar.  I was lucky, I survived.  Meeting Justin’s mom and dad, took me back to my childhood and those horrible nights, making me remember, and wondering how my own parents felt as I was growing up.  I know what it’s like from the child’s perspective, but I can’t imagine what it’s like from the parents perspective.  I’ve read articles, and seen stories, of kids and teens that leave us unexpectedly, but it’s never hit home like this for me.  I’ve never “felt” it so close like I do now.  I can’t make their pain go away, but when they told me about this concert, I couldn’t help but use my social network to do my best to get the word out for them.

Jammin 4 JustinI invite you to join Justin’s family & friends to celebrate his life on Saturday Jun 13th, 2015, while raising funds for a cure to type 1 diabetes.  This event is fully supported by JDRF Eastern Iowa Chapter.  ALL PROCEEDS from all ticket sales and all raffles, go to JDRF.

Speaking of raffles, there will be a raffle with some mind blowing prizes at this benefit.  Business supporters from across the Quad Cities region are donating amazing prizes to support this event.  The prizes just keep rolling in, but you’ll have to come to see what they are!  Now for the day’s schedule, which shapes up like this:

8:00AM Pancake Breakfast
9:00AM Jr. Bags Tournament
12:00PM Adult Bags Tournament
12:00PM Pretty Boy Floyd Meet & Greet
6:00PM Concert Begins

Jammin 4 JustinBands that are performing include Arianna Ferman featuring Shadow Stone, Canned Ham, Crop Circle, 9th Street Memory, Eleven Fifty Two, and 3 Years Hollow.  For those not in the music scene in the Quad Cities, those are the best bands in the area, and all are donating their time for this kickass show.  This is the going to the biggest event in the area this year!

Advanced Ticket’s are only $10, and you can get those by [CLICKING HERE].  The show will be located at a popular venue in Kewanee, IL called The Pioneer Club.  They are donating an incredible amount of time and resources to this event, so please show your support for them by liking their Facebook page [HERE]. Finally, if you use Facebook, we have a formal event with lots of pictures of raffle prizes and other news and info [AT THIS LINK].


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D&D and Diabetes

Dungeons & DragonsI’m a fanboy of Diabetic Danica, and she’s always posting about the interesting situations in which she encounters and makes friends with new type 1 diabetics.  Tonight I had such an encounter while playing Dungeons and Dragons (D&D) with a new group of people.

30 years ago I was very into role-playing and miniatures battles as a hobby.  There were a lot of different games that I played.  I was a teenager when I started, and I played through my mid twenties.  I grew out of it over time, and I hadn’t played in about 20 years, until this year.  I’ve been slowing re-entering the gaming world starting with Pathfinder 7 months ago, then tabletop board games and Vampire the Masquerade over the summer, and now X-Wing battles and D&D again this winter.  D&D is what got me started when I was 14.  Tonight was my first D&D game since I was oh, about 25.  I was stoked to play again, and I knew the dungeon master, but not the other 5  players.

If you’re not a gamer, you may not know that killing monsters makes you hungry.  So we’re all snacking around the table while we shoot arrows, cast spells, and clobber things.  I check my Dex as I’m eating some tasty barbecue chips, then look at the bag to get the carbs so I can bolus with my pump.  We were about half way through this dungeon crawl, hunting goblins and bugbears, when I look over at this young guy (early 20’s) who has a diabetic kit open with his insulin and syringes to bolus!  Instant bonding moment.  We forget about the goblins and start talking diabetes.  Then everyone else starts asking us questions about friends and family members who have diabetes.  The poor dungeon master (DM) didn’t know what to do.  LOL!  I pointed out that we could finish our diabetes talk at the end of the night, and got us back on track for the DM.  At the end of the night we had killed all the goblins, saved the hostage, and filled our pockets with loot.  We had a hell of time keeping our cleric alive, and he’s the one who’s suppose to heal the rest of us!

After the game, I invited him to our local support group, told him about the diabetic online community (#doc), and we talked for a while about our common condition.  He mentioned that he doesn’t really know many type 1 diabetics, and he’s interested in advocacy too.  So I can’t wait to introduce him to the online community, and help him get involved.   Isn’t it always just the coolest when this sort of thing happens?  The one place I’d NEVER expect to meet a fellow T1 is in a room full of gamer geeks.  Wicked cool.  Where’s the most interesting place you’ve ever met a fellow T1D?  Leave a comment!

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What Is Diabetes Awareness?

With November being diabetes awareness month, the online community is aflutter with “diabetes awareness” posts, but what IS diabetes awareness?  I think the meaning of that term lies in the eye of the beholder.  Some posts want you to be “aware” of diabetes, quoting statistics and such.  Some posts want you to understand what those with diabetes go through on a day to day basis.  Some posts pull at your heart strings with stories of people with diabetes battling to beat the disease.

What diabetes awareness means to ME is to make everyone, . . . I said EVERYONE, . . . A-W-A-R-E of the symptoms of diabetes. So you can save the life of a loved one that may not know they are diabetic. Even emergency room personnel, and even DOCTORS, don’t recognize diabetes symptoms. My goal with this diabetes awareness post, is to burn into your brain, these warning signs of diabetes. If you see any of these warning signs in a loved one, get them to a doctor, or an emergency room. Don’t screw around. It can save their life.


Urinating Often
Feeling Very Thirsty
Feeling Very Hungry (even though you are eating)
Extreme Fatigue
Blurry Vision
Cuts / Bruises That Are Slow to Heal
Rapid Unexplained Weight Loss (type 1)
Tingling, pain, or numbness in the hands/feet (type 2)

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Not another cure . . . . .

i-want-to-believeCure, schmure.  Not another cure.  I’m so sick of hearing about the “latest cure research” in diabetes.  I’ve been hearing about the latest cure research all my life.  We’ve been on the brink of a cure, all my life, and I’m still not cured.  This latest news story from Harvard Department of Stem Cell and Regenerative Biology, regarding creation of pancreatic insulin producing beta cells, from stem cells, is no different.  I’m just not excited about it.  I’ll be excited when I’m cured, not before.

Even IF there’s ever a cure, I don’t believe it will be offered to us.  Diabetes is the biggest recurring revenue source for big pharma, in the world.  A long lifetime of recurring revenue can be bled from nearly 30 million people, ever year, by multiple companies who supply diabetic supplies. Hell, if they cure diabetes, our economy will crash.

All of this hype about this latest cure news reminds me of the X-Files.  Fox Mulders basement office.  You remember the poster on his wall?  The UFO hovering with the quote “I want to believe”?  Basically, I desperately hope I”m 200% wrong, but I know better.  The definition of insanity is doing the same thing over and over, expecting a different result.  All my life, we’ve been on the brink of cure.  All my life, new research shows it’s right there, in sight, on the horizon.  I’m still not cured.  44 years as a T1D and I’m still not cured.  Seems a little insane to think this one is any different.  You can just call me Scully I guess.  She was always the sceptic, right?

Now many of my friends and family have personally sent me the link to the numerous news stories about this, and it took me forever to even go look at it, but I want you all to know how much I appreciate that you cared enough to share what you found.  I have read many articles now, and even tried to read the actual study, but it seems you need medical credentials to see that text.  Yes it looks hopeful, so thank you.

For those of you who have not yet seen this story, here is the direct link to the Harvard website:  http://hsci.harvard.edu/news/stem-cells-billions-human-insulin-producing-cells

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You Don’t Look Sick?

richthediabetic-gazeI have been uninspired to blog for a little while now.  The Diabetes Hands Foundation asked me to help them on a project recently, which inspired me to write this blog.  Thanks DHF.  I needed a good kick in the ass.  I’d like to point out right away that I’m not writing this today because anyone has accused me of not being sick.  It’s because I realize, that to others I don’t look sick, yet inside, mentally and physically, I am.  I think that for the first time in MANY years, I am experiencing a form of diabetes burnout (I can’t believe I’m admitting that here), and it’s affecting my mental state too.  So I’m going to write this blog in the hopes that it motivates me and makes me understand myself, so that I can turn things around the way I always used to.

When you meet me, I look like any other average 45 year old.  What you can’t see is the scar on my chest from emergency open heart surgery, that was caused by my diabetes.  You can’t see the 3 weeks of recovery it took to be able to walk again.  You can’t see the 3 months of cardiac rehab.  You can’t see YEARS of re-education it took to try to prevent that from ever happening again.  You can’t see the sweat from all the workouts to get myself healthy.  Most importantly, you can’t see the emotions I feel every time I look in the mirror at my broken body.

When you meet me, what you can’t see is the tingling and pain I feel in my feet and toes. The neuropathy caused by over 40 years of high blood sugars.  You weren’t there the first time I got out of bed, and fell down because I couldn’t feel my feet.  You can’t see the self doubt I feel, and the depression it causes, because if I had been more diligent, I may not have this complication of diabetes yet. You can’t see the fear that fills my mind every day that I will someday be “disabled”, and unable to walk.

When you meet me, you can’t see the burning I feel in my body when my blood sugar is high, or the inability to think that I get when my blood sugar is low.  You can’t see the seizures I’ve had as a child from hypoglycemia, or see the memories I have of seizures that should have killed me as an adult.  You can’t feel the burning of lactic acid that I have RIGHT NOW in my muscles because of the acidosis caused by high blood sugar.  (Don’t worry, I’ve got it under control . . . now.)

When you meet me, you can’t see that when I look at food, I don’t see food, I see math. The math of ((carbs – fiber / carb ratio) * fat grams = units of bolus insulin + (superbolus of basal insulin * number of hours basal is disabled)) When you look at pizza or cheesecake, you see pleasure.  What I see is guilt, because it’s nearly impossible for me to get that diabetic algebra calculation correct so that in 3 hours my blood isn’t 400 or 40, and 400 I can live with for a little while, where 40 will make me unconcious, but I know that 400  leads to more numbness in my feet, or future blindness, or possible kidney failure a few years down the road.

When you meet me, you can’t see the underlying depression I experience.  Knowing that my death will be a long slow death of multiple complications.  Knowing that eventually, I won’t be able to feel my feet at all.  Knowing that the only way to postpone this fate, is to get back on the wagon and become diligent again, but being completely uninspired to.

Yeah, I don’t look sick, but  . . . . .  live a lifetime in my shoes, and you’ll understand.

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mySugr Challenge Group Recap

frankLast week I led 4 type 1 diabetic friends in a mySugr challenge group on Facebook.  [Click here to learn more.]  I did this because “I” needed motivation, and it’s seemed to cause many in the #doc to want to run challenges of their own.  That’s so cool.  It definitely did the trick for me.  It got me focusing my attention on everything I needed to.

For me, what participating in the challenge did was it made me feel like I wanted to provide a good example, so I was more diligent in checking my blood sugar, and doing correction bolus’s.  It allowed me to see how much insulin I was dosing for all those carbs I was eating!  Holy cow!  That caused me to eat fewer carbs, leveling out that trend line in the app.  It let me see first hand how many hypers/hypos I had in the last 7 days, which was kinda upsetting.  It made me try harder to keep them to a minumum for the second half of the week, which worked!  These are just some of things that helped me.  Now I’d like to share what other challengers have said about being in the challenge group.

“It helped me focus for 3 straight days. It made me focus on what I’m doing in a more structured way. It confirmed how long my digestion is often taking to kick in which helps me have more confidence in what I’m trying . . . “

gerald“It’s very difficult to give constructive criticism on something that seems so perfect, so fun and so exciting! I only have the free version so I have not been able to experience the awesomeness of the full app. I do plan on purchasing this app and recommending it to EVERY pwd that I know.”

“What I like about the challenge group is the feeling of “I need to stay on top of things”. Whether it’s making sure to check BG before meals or when I felt high/low, lasering in on carb-counting, or simply just checking in with my moods and extra-curricular activities, I was able to keep track of trends a little better.”

I’ve been asked to try to think of recommendations for the mySugr team, but like one of my friends above said, it’s hard to find constructive criticism for mySugr when it’s so perfect the way it is.  I too plan on purchasing the full version of the app.  The only thing I can really suggest is perhaps adding a couple more free challenges so that we advocates can have options for running more challenges to get people excited about using mySugr, and improving their diabetes control.  Maybe a 3 day and a 5 day challenge.  Oh yeah, and if you wanted to name them after famous vampires, that would be totally cool.  😉




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How To Host A mySugr Challenge Group

mysugr-animatedmonsterSo this week I’ve been doing a test run of a mySugr challenge group on Facebook.  A 7 day challenge, who’s purpose is to make tracking your diabetes fun, while developing better tracking habits.  mySugr is a FREE diabetes management app for iPhone and Android, and it is hands down the absolute best diabetes app I have ever used.  My CDE has people download it and register while they’re in her office because she believes in it so much.  So far the response to this challenge group has been astounding.  Everyone is engaged, tracking, comparing, learning, joking, and more.  It’s been so much fun, and we’re only on day 3.  We’re a bunch of full grown adults that sit there tapping on the monster icon, to see what funny noises it will make.  You not only get a pet monster, but you also gain insights into your diabetes.  Pretty cool huh?  Yeah, mySugr rocks.

So here is a little template for how I’m running this challenge group.  First, you have to prospect for who wants to participate.  I suggest a few posts on your social networks and include this video with some of those posts for people who don’t know what mySugr is: Diabetes Companion App  You’ll want to keep the challenge group small.  5 or 6 people works great, but an absolute max of 10 people.  I suggest you start with a short challenge of 7 days.  Define the start and stop days.  I did my first one from Sunday through Saturday.

Once you have your list of challengers, create a SECRET Facebook group.  This keeps all group posts hidden for the challengers privacy.  Then customize the group if you want, and invite your challengers to the group.  If they’re not on your friends list, you can add them via email.

Now each challenger will be expected to post a screenshot of their mySugr overview screen or logbook at the end of each day (or the start of the next).  If they want to ask for advice they can, or they can share their wins and losses.  Jump for joy, or ask for a hug.  Your responsibility is to watch who’s not checking in, and go ask if everything is ok, or if they just forgot.  Don’t be annoying, just be a coach.  Let them know you care by checking in with them if you don’t hear from them.

You as the leader/advocate will also want to post daily motivation and information.  I recommend 1 or 2 posts each day.  I’ve been posting videos from the mySugr YouTube channel to help them get to know the app better, and let them know it’s benefits and options.  Below I’ve created a list of posts that you could use for each day to give you starting point.


Make sure to sign up for the free ENDURANCE challenge in your app’s settings screen to support JDRF: http://youtu.be/1IL7h9GY41k?list=PLKhlz-YOvffH1hsRrxkiwhu7ZZ1Ws7T4w

Don’t forget to name your diabetes monster!  What will you name yours?


Check out this motivational video from mySugr as you learn more about mySugr Companion: http://youtu.be/1IL7h9GY41k?list=PLKhlz-YOvffH1hsRrxkiwhu7ZZ1Ws7T4w

The more you track in the app, the more points you earn.  The more points you earn, the faster you tame your monster.  Who’s tamed their monster already?!

DAY 3 

Scott gives us an overview of the mySugr Companion and how to get the most out of it: http://youtu.be/LonCbUbIup0?list=PLKhlz-YOvffH1hsRrxkiwhu7ZZ1Ws7T4w

If you’ve sat there repeatedly tapping your diabetes monster, just to hear the funny sounds it makes, and watching the goofy dances it does, then fess up here.  ADMIT IT!!!  😉


Fredrik explains the integration of mySugr Companion and BGstar / iBGstar blood glucose meters: http://youtu.be/QGdkTX1NDn4?list=PLKhlz-YOvffH1hsRrxkiwhu7ZZ1Ws7T4w

What has mySugr helped you to discover about your diabetes this week?  What insights have you gained as a result of using it?


Fredrik shows us the value of the reports function of mySugr Pro, and how practical they are for your diabetes care team: http://youtu.be/p4nt1ghFxg4?list=PLKhlz-YOvffH1hsRrxkiwhu7ZZ1Ws7T4w

Raise your hand if you think this challenge group is causing you to track more about your diabetes than you would otherwise.  What do you like most about mySugr so far?


From now on, cables are a thing of the past with mySugr Importer: http://youtu.be/vQkD1HU3MLk?list=PLKhlz-YOvffH1hsRrxkiwhu7ZZ1Ws7T4w

Did you know that diabetes advocate and blogger Scott Johnson is the mySugr lead contact in the US?  Connect with the mySugr team at this link: http://mysugr.com/team/


Here’s a final review of the mySugr Companion app:  http://youtu.be/BTWqq1EZWFs?list=PLKhlz-YOvffH1hsRrxkiwhu7ZZ1Ws7T4w

What did you like most about participating in this challenge group?  Will you be getting mySugr pro?  Oh! Don’t forget to go give mySugr 5 stars in the app store!


So that’s the basics of running a mySugr challenge group.  If you decide to run one yourself please leave a comment below and let me know!  I’d love to hear how it goes.





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A mySugr Challenge Group

mysugr companion juniorDo you know what mySugr is?  (Yes, that’s how it’s spelled.)  If not, it’s a great diabetes management app, unlike anything you’ve ever seen.  Watch the video below to get an idea of why it’s so awesome.  Well, today is the start of our local Quad Cities adult type 1 diabetes support group‘s mySugr challenge.  What does that mean?  Well, when I used to be a Beachbody coach, we would run “challenge groups” for the different programs like P90X3 and T25.  Small support groups of less than 10 people, for motivation.  It was done through FB, by creating a private group, and inviting everyone into that group.  Then each day, I would post videos, tips, motivational quotes, etc.  All of the challengers were expected to report in each day that they did their workout and kept to their diet.

So for this mySugr challenge, 5 of us are committing to use mySugr for 7 days straight, to record our blood sugars and carbs (more if they want to).  At the end of each day, we’re going to post screenshots of our mySugr overview screen, and then post about our struggles and our wins.  If someone doesn’t report in for that day, they get tagged and we ask them if they’re ok, or if they just forgot to post.  My responsibility is just to post daily helpful info.  Maybe a blog I read that applies to what we’re doing, or videos or product info about a mySugr feature not everyone is a aware of.  See how that works?  It’s fun!  You should try it with your local group!  This is kind of a trial run.  Just 7 days, to see if people like it.  If they like it, the next step is to run a 21 day challenge, since it takes 21 days to create a habit.  I’ll blog about this again next week to share what our results are, and any insights we had as a result of doing this.




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FDA Basics for Diabetes Advocacy

masterlabIt seemed to me that most of the effort for the MasterLab was to teach advocates like me how to effect change on the hill in Washington.  Whether it be in Congress or the FDA.  They had a great presentation from Stayce Beck of the FDA explaining the approval process for medical devices like our pumps, cgms, and blood glucose meters.  She was conveying a great deal of info, and using acronyms and terms I didn’t understand.  As I sat there, I thought I couldn’t be the only person that was a little lost, so I’ve been trying to educate myself on the FDA approval process.  Below is a short breakdown in layman’s terms of what I’ve learned.  If I’m wrong about anything, please leave a comment.  I’m certainly no expert, but wanted to share what I’ve learned.

Congress passes LAWS, but executive agencies like the FDA, which are created by congress, issue RULES.  Both laws and rules seem to have the same legal effect.  Congress has little to do with RULE making, but they do have the ability to overturn, or stop a rule from being created, as does the President.

Both the FDA and YOU, the constituent have the ability to create a proposed rule.  The process of creating a RULE, is that a “draft of proposed rule” is created and sometimes submitted to the president for review.  Then it’s created in the Federal Register, an electronic database and webpage, where the details of the rule are explained.  This also triggers the notification to the public of the proposed rule, and the opportunity for the public to comment, which usually lasts 60 days (but that time frame isn’t set in stone).  Once created in the federal register, it’s known as a “docket”.  Stayce explained that this is a very important part of the rule making process.  When we comment, it makes a difference.  Especially when we ALL COMMENT.  Then after the comment period passes, the FDA decides whether to submit a new proposed rule with changes, or go ahead and create a “draft final rule”.  Next, it’s sent to the president for review, and then to congress.  If they don’t disapprove the draft final rule, it becomes a final rule at which point it is entered into the Federal Register and the Code

These 2 documents really helped me understand this process.  For more details about this process, first read this Rule Making Process PDF, then read this Federal Register Tuturial.  Finally, to try to keep up on what the FDA is doing, go to their homepage where you can find links to RSS feeds, how to connect with them on social media, and sign up for their email newsletters.  The link is http://www.fda.gov/.

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Diabetes Advocates – MasterLab #masterlab #cwdffl14

masterlab2 days ago, on 02 Jul 2014, I attended the Diabetes Advocates MasterLab seminar at the Children With Diabetes – Friends For Life conference in Orlando, FL.  I was able to attend this seminar thanks to a scholarship from the Diabetes Hands Foundation – Diabetes Advocates (DHF), and Novo Nordisk.  A sincere thank you to everyone at DHF for all the work done in organizing this event, and organizing our travel arrangements.  Words seem insignificant in expressing my appreciation.  THANK YOU.  Also a very big thank you to Novo Nordisk for the scholarship money that allowed these scholarships to be offered to the diabetes advocates program.

The Master Lab seminar was a 1 day intensive seminar designed to make those in the Diabetes Advocates program, more effective advocates.  It provided us with tools and information to teach us how to actually effect change in Washington with the FDA.  We heard from policy makers, from advocates that have built movements, from a panel of people that explained exactly how to talk to your senators and representatives, and much more.  I can’t even explain how valuable this training was.  In the coming days and weeks, I will be releasing blogs, videos, tweets, all with the purpose of sharing what I learned.

It was so nice to meet so many of my mentors in the advocacy world too.  People I look up to.  People I didn’t realize were fans of my blog.  Diabetic celebrities.  I met so many people.  It makes me want to play all of my vacation next year for diabetes conventions.

I want to leave you with a quote from the keynote speaker of the day at Master Lab.  His name is Paul Madden, and he’s the Senior Director of the diabetes program at Project Hope.  He said “I don’t wait for them to cure it. I go on with my life.”

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